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Evaluating Dashboard-Integrated Pharmacist-Led Education on Improving Sacubitril/Valsartan Adherence in Heart Failure (PharmD ASSIST HFrEF)

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National Taiwan University

Status

Not yet enrolling

Conditions

Medication Adherence
Sacubitril/Valsartan
Heart Failure With Reduced Ejection Fraction (HFrEF)

Treatments

Device: interactive visualization dashboard (the Enhancing Sacubitril/valsartan Adherence from Initiation to Continuation [ESAIC] dashboard)

Study type

Interventional

Funder types

Other

Identifiers

NCT06900803
202501197RINC

Details and patient eligibility

About

The goal of this pragmatic clinical trial is to evaluate whether pharmacist-led education, integrated with interactive visualization dashboards, can enhance medication adherence in patients with heart failure who are prescribed sacubitril/valsartan. The main question it aims to answer is: Can pharmacist-led interactive visualization dashboards improve adherence to sacubitril/valsartan compared to usual care without the dashboard intervention?

Researchers will compare patients receiving pharmacist-led education with interactive dashboards to those receiving standard education, assessing differences in medication adherence and clinical outcomes, among others.

Participants will:

  • Complete baseline and follow-up questionnaires on medication adherence and satisfaction with pharmacist-provided services, and others.
  • Engage in education sessions led by pharmacists, with or without dashboard integration.

The study outcomes will include medication adherence, and secondary outcomes such as patient satisfaction with pharmacist-provided services, optimized guideline-directed medical therapy score, time to high medication adherence, the calculated proportion of days covered, New York Heart Association functional classification, and the net promoter score used for evaluating recommendation and satisfaction with the dashboard intervention.

Enrollment

200 estimated patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • adults aged 20 or older
  • a diagnosis of HFrEF, which is defined by a left ventricular ejection fraction of 40% or less
  • currently receiving sacubitril/valsartan at the time of recruitment
  • receiving care at the cardiology department or cardiology ward at National Taiwan University Hospital
  • referral from the clinicians at National Taiwan University Hospital

Exclusion criteria

  • unable or unwilling to provide informed consent, adhere to study protocols, or complete required questionnaires in person during three scheduled visits (i.e., 3, 6, 12 months after the baseline measurement)
  • having received care at the pharmacist-led HF clinic at National Taiwan University Hospital

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 4 patient groups

Low Adherence Cluster - Intervention Group
Experimental group
Description:
Dashboard interventions integrated into pharmacist-led education in the low adherence cluster
Treatment:
Device: interactive visualization dashboard (the Enhancing Sacubitril/valsartan Adherence from Initiation to Continuation [ESAIC] dashboard)
Low Adherence Cluster - Control Group
No Intervention group
Description:
Pragmatic pharmacist-led education, without dashboard interventions, in the low adherence cluster
High Adherence Cluster - Intervention Group
Experimental group
Description:
Dashboard interventions integrated into pharmacist-led education in the high adherence cluster
Treatment:
Device: interactive visualization dashboard (the Enhancing Sacubitril/valsartan Adherence from Initiation to Continuation [ESAIC] dashboard)
High Adherence Cluster - Control Group
No Intervention group
Description:
Pragmatic pharmacist-led education, without dashboard interventions, in the high adherence cluster

Trial contacts and locations

0

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Central trial contact

Wan-Tseng Hsu, PhD; Tung-Chun Russell Chien, PharmD

Data sourced from clinicaltrials.gov

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